Cinnamyl benzoate (CAS 5320-75-2) — Balsamic Base Note Fragrance Ingredient

Balsamic · Sweet

Cinnamyl benzoate

CAS 5320-75-2

Origin
synthetic
Note
Base
IFRA
Generally safe
Data as of: Apr 2026

What Is Cinnamyl benzoate?

Cinnamyl benzoate is a synthetic fragrance ingredient that adds warm, balsamic notes to perfumes and scented products. You’ll find it in oriental fragrances, soaps, and candles. This molecule matters because it provides long-lasting sweetness without being overpowering, acting as a bridge between top notes and deeper base accords.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major restrictions
Potential skin sensitivity at high concentrations
CAS
5320-75-2
Formula
Mixture
MW
Variable
Odor Family
Balsamic · Sweet
Layer 1 · Enthusiast

What Does Cinnamyl benzoate Smell Like?

Cinnamyl benzoate unfolds like liquid amber – opening with a soft cinnamon warmth that quickly melds into honeyed benzoin resin. The dry-down reveals a velvety vanilla-tinged sweetness that lingers close to the skin. Imagine the scent of sun-warmed antique wood furniture polished with beeswax, or the faint aromatic trail left by aged liqueur barrels.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Shalimar(Guerlain, 1925)

Used as a balsamic modifier to enhance the vanilla-oriental base, adding warmth and diffusion without overpowering the delicate citrus top notes.

Opium(Yves Saint Laurent, 1977)

Provides a smooth transition between the spicy carnation heart and benzoin base, creating the signature ‘amber glow’ effect.

Cinnabar(Estée Lauder, 1978)

Works synergistically with patchouli to create the fragrance’s namesake cinnamon-spiced resinous character.

Layer 2

2D Molecular Structure

3-Phenylprop-2-en-1-yl benzoate

SMILES: O=C(OCC=CC1=CC=CC=C1)C1=CC=CC=C1

Chemistry, Properties & Perfumer Guide

The Chemistry

Cinnamyl benzoate is an ester formed from cinnamyl alcohol and benzoic acid. While theoretically occurring in nature, commercial production is exclusively synthetic via esterification reactions. The molecule’s planar structure allows excellent blending properties with both polar and non-polar fragrance materials. Its moderate molecular weight contributes to good substantivity on skin.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Boiling Point~300 °C (estimated)
Density~1.05 g/cm³ (estimated)

Perfumer Guide

Note Position
Base
Volatility
Low (8+ hours)
Blending
Excellent
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Base note fixative
Soap0.1-0.5%Up to 1%Stable in alkaline systems

Classic Accords

+ Vanilla + Labdanum = Oriental + Sandalwood + Patchouli = Woody-Amber

Tip: Use with ionones to create seamless floral-amber transitions.

Alternatives & Comparisons

1
Benzyl benzoate CAS 120-51-4

Lighter alternative with similar fixative properties but less balsamic character.

2
Cinnamyl cinnamate CAS 122-69-0

More intense cinnamon-spice profile for stronger oriental compositions.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

General reference only. Consult current IFRA Standards Library before formulating.

IFRA Status

No IFRA restrictions (as of Amendment 49).

RIFM Assessment

RIFM assessment confirms safe use at current industry levels.

Sustainability

As a synthetic material, cinnamyl benzoate production avoids harvesting of natural resources. Modern manufacturing processes minimize solvent waste through efficient esterification methods. The material’s longevity in fragrance reduces reapplication needs in finished products.

Explore Cinnamyl benzoate

Browse essential oils and aroma compounds.

Browse on iHerb →

Affiliate disclosure: we may earn a small commission at no extra cost to you.

References

  1. Bauer, K. et al. (2001). Common Fragrance and Flavor Materials. Wiley-VCH.

Data: PubChem (NIH), PubMed, RIFM, IFRA. Last reviewed: Apr 2026.

Report a data error

Ingredient Data Sheet

CAS 5320-75-2

Physical Properties

Molecular Weight238.28 g/mol🔬 PubChem
LogP (Octanol-Water)4.6🔬 PubChem
Boiling Point351 °C🔬 EPA CompTox
Vapor Pressure0 mmHg @ 25°C📊 OPERA
Flash Point176.1 °C🔬 EPA CompTox
log Kp (skin permeability)-0.888💻 Calculated
SMILESC1=CC=C(C=C1)C=CCOC(=O)C2=CC=CC=C2🔬 PubChem

Volatility & Performance

Fragrance NoteBase💻 Calculated
Volatility ClassVery slow💻 Calculated
Persistence Score11.4 / 5💻 Calculated

Odor & Flavor

Primary Descriptorsbalsamicspicysweet• leffingwell
Functional Groupsesteretheralkenearomatic💻 RDKit
“Mild-spicy, tenacious and balsamic odor. Freshly prepared and pure grade materials are odorless to many people, faintly "musk" to others.”📖 Arctander
Cinnamyl benzoate has a characteristic balsamic, aromatic, spicy odor.📖 Fenaroli

Flavor Notes (Arctander)

“Used in flavor compositions for imitation Butter, Caramel, Raspberry and in a multitude of Fruit flavors.”📖 Arctander

Regulatory Status

IOFI ClassificationNature Identical📖 Fenaroli
Data Sources & Attribution
Physical data: PubChem (NIH/NLM), U.S. EPA CompTox Dashboard, EPA OPERA models, RDKit. Odor & flavor: Arctander (Perfume & Flavor Chemicals), Fenaroli's Handbook of Flavor Ingredients, Leffingwell. Thresholds: van Gemert (Compilations of Odour Threshold Values). Regulatory: IFRA Standards 51st, FEMA GRAS. Trade names: Surburg (Common Fragrance & Flavor Materials). All data compiled and cross-referenced for perfumertools.com.

Physicochemical Properties

DTXSID: DTXSID1052169

Physical Properties

Molecular Weight 238.286 g/mol🔬 EPA CompTox
Density 1.12 g/cm^3📊 OPERA
Boiling Point 363.05 °C📊 OPERA
Melting Point 51.845 °C📊 OPERA
Flash Point 180.247 °C📊 OPERA
Refractive Index 1.607 Dimensionless📊 OPERA
Molar Volume 212.693 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 3.961 Log10 unitless📊 OPERA
LogD (pH 5.5) 3.961 Log10 unitless📊 OPERA
LogD (pH 7.4) 3.961 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 8.21 Log10 unitless📊 OPERA
Water Solubility 0 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0 mmHg📊 OPERA
Viscosity 9.396 cP📊 OPERA
Surface Tension 42.827 dyn/cm📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 26.3 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 2 count💻 Computed
Rotatable Bonds 4 count💻 Computed
Aromatic Rings 2 count💻 Computed
Molar Refractivity 73.487 cm^3/mol📊 OPERA
Polarizability 29.132 Å^3📊 OPERA

Data Sources:

🔬 EPA Experimental data from U.S. EPA CompTox Chemicals Dashboard & CTX APIs. 📊 OPERA Predicted using EPA's OPERA QSAR models. 💻 Computed Calculated from SMILES using RDKit.

Similar Posts